Last updated: 11/07/2018 07:08:42
Indirect comparison between eltrombopag & romiplostim
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Finalized
Finalized
Trial overview
Official title: Indirect Comparison of efficacy of treatments for idiopathic immune thrombocytopenic purpura - review of platelet responses and bleeding events
Trial description: An indirect comparison to compare the efficacy of eltrombopag versus romiplostim
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Durable response: platelet count of >=50 and <400 Gi/L
Timeframe: 6 months
Overall response: either a durable response or a transient platelet response
Timeframe: 6 months
Secondary outcomes:
Not applicable
Interventions:
Drug: Eltrombopag
Drug: Romiplostim
Drug: Placebo
Enrollment:
1
Observational study model:
Other
Primary completion date:
Not applicable
Time perspective:
Retrospective
Clinical publications:
Dwayne Boyers, Xueli Jia, David Jenkinson and Graham Mowatt . Eltrombopag for the Treatment of Chronic Immune or Idiopathic Thrombocytopenic Purpura. [Pharmacoeconomics]. 2012;30(6):483-395.
Medical condition
Thrombocytopaenia
Product
eltrombopag
Collaborators
Not applicable
Study date(s)
August 2009 to June 2011
Type
Observational
Phase
Not applicable
Participation criteria
Sex
Female & Male
Age
18+ years
Accepts healthy volunteers
No
- Adults with ITP
- Pre-specified treatment
- Adults with ITP for other reasons
Inclusion and exclusion criteria
Inclusion criteria:
- Adults with ITP
- Pre-specified treatment
- Prospective clinical studies with at least 10 patients
Exclusion criteria:
- Adults with ITP for other reasons
Trial location(s)
No location data available.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Refer to study documents
Recruitment status
Finalized
Actual primary completion date
Not applicable
Actual study completion date
2011-09-06
Plain language summaries
Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.
Additional information about the trial
Not applicable
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